Cyclosporine on Day Zero as Prophylaxis for Cytokine Release Syndrome
Primary Purpose
Stem Cell Transplant Complications, Cytokine Release Syndrome
Status
Unknown status
Phase
Phase 2
Locations
Mexico
Study Type
Interventional
Intervention
Cyclosporine
Sponsored by
About this trial
This is an interventional prevention trial for Stem Cell Transplant Complications focused on measuring Cyclosporin, Haploidentical, Outpatient
Eligibility Criteria
Inclusion Criteria:
- Patients between 16-60 years of age who receive their first haploidentical transplant.
Exclusion Criteria:
- Patients positive for the human immunodeficiency virus (HIV), Hepatitis B or C virus
- Pregnancy or lactation
- Patients with documented infection at the time of transplantation
- Presence of previous autoimmune diseases
- Inability to tolerate the oral route
Sites / Locations
- Hospital Universitario Dr. José E. González, Centro Universitario contra el CáncerRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Arm 1
Arm 2
Arm Description
Cyclosporine 6 mg/kg orally divided into two doses per day starting in the morning on day 0 after transplantation, mycophenolic acid 1 gram orally (2 tablets 500 mg) from day 0 post-transplant and PT-CY at 50 mg/kg per day on day +3 and +4.
Cyclosporine 6 mg/kg orally divided into two doses per day starting in the morning on day +5 of the transplant, mycophenolic acid 1 gram orally (2 tablets of 500 mg) from day +5 post-transplant and post-transplant cyclophosphamide (PT-CY) at 50 mg/kg per day on days +3 and +4
Outcomes
Primary Outcome Measures
Cytokine Release Syndrome
Presence of Fever, hypotension, hypoxemia
Secondary Outcome Measures
Full Information
NCT ID
NCT04781803
First Posted
March 1, 2021
Last Updated
March 3, 2021
Sponsor
Hospital Universitario Dr. Jose E. Gonzalez
1. Study Identification
Unique Protocol Identification Number
NCT04781803
Brief Title
Cyclosporine on Day Zero as Prophylaxis for Cytokine Release Syndrome
Official Title
Cyclosporine on Day Zero as Prophylaxis for Cytokine Release Syndrome in Outpatient Haploidentical Hematopoietic Stem Cell Transplantation
Study Type
Interventional
2. Study Status
Record Verification Date
March 2021
Overall Recruitment Status
Unknown status
Study Start Date
March 25, 2021 (Anticipated)
Primary Completion Date
January 17, 2023 (Anticipated)
Study Completion Date
February 17, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Universitario Dr. Jose E. Gonzalez
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Phase II, randomized controlled, unblinded clinical trial. Will evaluate whether the administration of oral cyclosporine started on day 0 of transplantation is effective in reducing the incidence of cytokine release syndrome (CRS) in patients who receive an outpatient haploidentical transplant.
Detailed Description
CRS is usually limited after the administration of post-transplant cyclosporine (PT-CsA) administered on days +3 and +4, however, there is no standard prevention or treatment regimen for CRS after haplo-TCPH and therapeutic behavior has usually been adopted.
Sample of 32 patients between the ages of 16 and 60 who receive their first haploidentical transplant at our center. In the control group, CsA 6 mg/kg orally divided into two doses per day starting in the morning on day +5 of the transplant, mycophenolic acid 1 gram orally (2 tablets of 500 mg) from day +5 post-transplant and post-transplant cyclophosphamide (PT-CY) at 50 mg/kg per day on days +3 and +4 and in the experimental group, CsA 6 mg/kg orally divided into two doses per day starting in the morning on day 0 after transplantation, mycophenolic acid 1 gram orally (2 tablets 500 mg) from day 0 post-transplant and PT-CY at 50 mg/kg per day on day +3 and +4.
Will document the presence of CRS and its degree, as well as the need for hospitalization, associated infectious processes, and a day to recover neutrophils and platelets. Additionally, 4 blood samples will be taken from the patients to determine the level of cytokines and C-reactive protein.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stem Cell Transplant Complications, Cytokine Release Syndrome
Keywords
Cyclosporin, Haploidentical, Outpatient
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
32 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Arm 1
Arm Type
Experimental
Arm Description
Cyclosporine 6 mg/kg orally divided into two doses per day starting in the morning on day 0 after transplantation, mycophenolic acid 1 gram orally (2 tablets 500 mg) from day 0 post-transplant and PT-CY at 50 mg/kg per day on day +3 and +4.
Arm Title
Arm 2
Arm Type
No Intervention
Arm Description
Cyclosporine 6 mg/kg orally divided into two doses per day starting in the morning on day +5 of the transplant, mycophenolic acid 1 gram orally (2 tablets of 500 mg) from day +5 post-transplant and post-transplant cyclophosphamide (PT-CY) at 50 mg/kg per day on days +3 and +4
Intervention Type
Drug
Intervention Name(s)
Cyclosporine
Intervention Description
Cyclosporine 6 mg/kg and mycophenolic acid 1 gram orally on day 0 post-transplant
Primary Outcome Measure Information:
Title
Cytokine Release Syndrome
Description
Presence of Fever, hypotension, hypoxemia
Time Frame
day 0 to day 30
10. Eligibility
Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients between 16-60 years of age who receive their first haploidentical transplant.
Exclusion Criteria:
Patients positive for the human immunodeficiency virus (HIV), Hepatitis B or C virus
Pregnancy or lactation
Patients with documented infection at the time of transplantation
Presence of previous autoimmune diseases
Inability to tolerate the oral route
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Perla R Colunga-Pedraza, MD
Phone
528183488510
Ext
378
Email
colunga.perla@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Julia Colunga-Pedraza, MD
Phone
528183486136
Ext
435
Email
julia_ecp@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Oscar González-Llano, MD
Organizational Affiliation
Hospital Universitario ¨Dr. José Eleuterio González
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Universitario Dr. José E. González, Centro Universitario contra el Cáncer
City
Monterrey
State/Province
Nuevo Leon
ZIP/Postal Code
64460
Country
Mexico
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Perla Colunga-Pedraza, MD
Phone
+5218110761973
Email
colunga.perla@gmail.com
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Cyclosporine on Day Zero as Prophylaxis for Cytokine Release Syndrome
We'll reach out to this number within 24 hrs